Tag | Content |
---|
EnhancerAtlas ID | HS139-20128 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr16:2748550-2749820 |
Target genes | Number: 19 | Name | Ensembl ID |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr16:2749086-2749097 | CATGAGTCACC | - | 6.62 | JUN(var.2) | MA0489.1 | chr16:2749087-2749101 | ATGAGTCACCACCT | - | 6.13 | JUND | MA0491.1 | chr16:2749086-2749097 | CATGAGTCACC | - | 6.02 | Tcf12 | MA0521.1 | chr16:2749640-2749651 | CAGCAGCTGTT | - | 6.32 | ZNF740 | MA0753.2 | chr16:2748591-2748604 | CCGCCCCCCCCAC | + | 7.82 |
|
| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_08752 | chr16:2748839-2750408 | Brain_Inferior_Temporal_Lobe |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr16 | 2748986 | 2749233 | chr16 | 2749393 | 2749740 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH16I002699 | chr16 | 2749541 | 2749690 |
|
Enhancer Sequence | TGCTGGGCCT TGGGCATCAG TCCCGTCCCT GAGAGCTGAG CCCGCCCCCC CCACCCAAGC 60 TCAGCTCCCT TGAGAAGGCA CCAGGAGTGG GGTGTGTGCC GCACTGTGGC CGCGGCTGCC 120 ATCAGAAGTC TCGGTCCACG TAGAGCCCTG GGCCCTGTGC AGACGCTCCT AGCCTGGCCG 180 CTCAGGGCCG CTGGCCACCT AGCGACTTGC CCAGTTCCCC CTCCTGCTGG AGCTCCCTTG 240 GTGCCACTGA GGGATCTGGA GGGGCTCCTT GTCTGTGGGG CAGGAGCTGC GTCCCGCGCC 300 CCGGGTCACC TTGTCCAGTC TGCTTTTTTC CCTGTTGTGT GACCGGGCTG TGTGGGCACT 360 CCCTGCCTCA GTCTACCTAC CTGTATGACG CAGGTGGGCA GGAAATGGTG CAGGTGGGAG 420 AGTCTGCGGT CCAGCCTTGC TGTGACACAG TAGCATCTCA CTGTCTTGCA GAATAAAGCA 480 ACTCGGGCAT GTGACCTCGA GGCCACTGTG TGCCTTTGTC ACTCAGGCAT CCCTGGCATG 540 AGTCACCACC TTAAGGTCAG GGACCCAGGA CCTCTGAACC CCTTCTCACT GCTGCGTTTC 600 CGTCCAGCCC CGTCTGCAGC CTGAGTCCTC CGTAGTGACT GTCCAGGATG TGGGGCCACC 660 CCGCCCACTG GGGAGCAGCT CCATGCAGGC GGGCGGCCCT GGTGGCTCAC CATCACTCCC 720 AGGACCACAG CTGCCTGGAG GGGCACAGCA AGCGTGCCAG GCAGGTGGGG GATTAGGAGG 780 TGGATGGAGT TTTAGGAAGC AGCTCAGCCT TCGGGAGGCC CAAGTCCAGG CTGCCGCGCA 840 AGTTCAAGAG CCTTTTTCTG GTAGCTGGGA GCGAGCTTCG TCTGGCACTG GCTCTCAGGG 900 CCCTGCTTGC CAGAGCCTTT CCCGACCGAT GAATTCAGGG CTGCACGGTT GCTGCGTGCG 960 GAGCAGACGT GGACGCTCTC GTGTCGTCAT GTCGAGCCAC AGGTGCTCTT GGGATTTCAG 1020 GAACATGACT CATTTTATTT TGGAACTTAG AAATAGAAAT ATTTTTGGAG GCGAACGAGG 1080 AAGCAGAAAA CAGCAGCTGT TCGGGCCGCG TGTTTTGCTT TTGTGGATGT GCTCAGGATT 1140 GCTTTGGGCC TCGTGCCCTG TGCTGAGAAC TGCAGAGTGG ACCTCAGCCT CCCTGGGTCA 1200 CCTGGGCTGG GGCCACAGGC AGCAGTGGGA CATGGGTGGC CCGCCCTTAC CTGTGCCCAT 1260 TGTCCTTGCA 1270
|